Consequences of TIPSS placement on the body composition of patients with cirrhosis and severe portal hypertension: a large retrospective CT-based surveillance.


Journal

Alimentary pharmacology & therapeutics
ISSN: 1365-2036
Titre abrégé: Aliment Pharmacol Ther
Pays: England
ID NLM: 8707234

Informations de publication

Date de publication:
11 2020
Historique:
received: 04 03 2020
revised: 31 03 2020
accepted: 19 08 2020
pubmed: 16 9 2020
medline: 20 1 2021
entrez: 15 9 2020
Statut: ppublish

Résumé

Body composition may be modified after improvement of portal hypertension (PHT) by transjugular intrahepatic portosystemic shunt (TIPSS) insertion. To evaluate changes in body composition following TIPSS placement, their relationship with radiological TIPSS patency and function, and the predictive value of these parameters METHODS: We retrospectively included 179 patients with cirrhosis who underwent TIPSS placement in our centre for severe PHT from 2011 to 2017. CT scan-based surveillance was performed at baseline, 1-3 (M1-M3) and 6 months (M6). The median model for end-stage liver disease (MELD) score was 11.4 (8.8-15.1) and Child-Pugh score 8 (7-9). Only the MELD score (HR 1.14, 95% CI 1.08-1.20) and sarcopenia assessed by transversal right psoas muscle thickness at the umbilical level/height (TPMPT/height) (HR 0.86, 95% CI 0.79-0.96) were independently associated with 6-month mortality on multivariate analysis. After TIPSS insertion, TPMT/height increased from 19 mm/m (baseline) to 19.6 mm/m (M1-M3, P = 0.004) and 21.1 mm/m (M6, P < 0.0001). The improvement and its extent were dependent on the radiological patency and dysfunction of TIPSS. Subcutaneous fat surface (SCFS) increased from 183.4 to 193 cm Sarcopenia is independently associated with 6-month outcome and improves after TIPSS placement, together with an inverse evolution of subcutaneous and visceral fat. TIPSS not only treats PHT but also improves body composition.

Sections du résumé

BACKGROUND
Body composition may be modified after improvement of portal hypertension (PHT) by transjugular intrahepatic portosystemic shunt (TIPSS) insertion.
AIMS
To evaluate changes in body composition following TIPSS placement, their relationship with radiological TIPSS patency and function, and the predictive value of these parameters METHODS: We retrospectively included 179 patients with cirrhosis who underwent TIPSS placement in our centre for severe PHT from 2011 to 2017. CT scan-based surveillance was performed at baseline, 1-3 (M1-M3) and 6 months (M6).
RESULTS
The median model for end-stage liver disease (MELD) score was 11.4 (8.8-15.1) and Child-Pugh score 8 (7-9). Only the MELD score (HR 1.14, 95% CI 1.08-1.20) and sarcopenia assessed by transversal right psoas muscle thickness at the umbilical level/height (TPMPT/height) (HR 0.86, 95% CI 0.79-0.96) were independently associated with 6-month mortality on multivariate analysis. After TIPSS insertion, TPMT/height increased from 19 mm/m (baseline) to 19.6 mm/m (M1-M3, P = 0.004) and 21.1 mm/m (M6, P < 0.0001). The improvement and its extent were dependent on the radiological patency and dysfunction of TIPSS. Subcutaneous fat surface (SCFS) increased from 183.4 to 193 cm
CONCLUSIONS
Sarcopenia is independently associated with 6-month outcome and improves after TIPSS placement, together with an inverse evolution of subcutaneous and visceral fat. TIPSS not only treats PHT but also improves body composition.

Identifiants

pubmed: 32931618
doi: 10.1111/apt.16080
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1516-1526

Commentaires et corrections

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Informations de copyright

© 2020 John Wiley & Sons Ltd.

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Auteurs

Florent Artru (F)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.
Service de gastroentérologie et d'hépatologie, Centre Hospitalier Universitaire Vaudois (CHUV), Lausanne, Switzerland.

Xavier Miquet (X)

Service de radiologie digestive, Hôpital Claude Huriez, CHU Lille, Lille, France.

Mustapha Azahaf (M)

Service de radiologie digestive, Hôpital Claude Huriez, CHU Lille, Lille, France.

Julien Labreuche (J)

Département de biostatistiques, CHU Lille, Lille, France.

Line Carolle Ntandja Wandji (LC)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

Géraldine Sergent (G)

Service de radiologie digestive, Hôpital Claude Huriez, CHU Lille, Lille, France.

Amélie Nobécourt (A)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

Pierre Toumelin (P)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.

Guillaume Lassailly (G)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

Sébastien Dharancy (S)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

Olivier Ernst (O)

Service de radiologie digestive, Hôpital Claude Huriez, CHU Lille, Lille, France.

Philippe Mathurin (P)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

Alexandre Louvet (A)

Service des maladies de l'appareil digestif, Hôpital Claude Huriez, CHU Lille, Lille, France.
U995 - LIRIC - Lille Inflammation Research Center, Université de Lille/Inserm/CHU de Lille, Lille, France.

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